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C-PRO - The Effect of Cross-sectorial Use of Patient-Reported Outcomes for Patients With Chronic Degenerative Shoulder Conditions
This research project aims to test if systematic (extensive) use of patient-reported outcomes across treatment boundaries can 1. improve patients' and health professionals' understanding of individual patients' conditions and health changes, 2. improve indications for treatment, 3. strengthen patient empowerment, and 4. reduce patients' utilization of health services. The study will be performed in the particular context of patients with chronic degenerative conditions of the shoulder. These patients are characterized by contact with numerous health professionals from different health sectors, such as general practitioner, physiotherapists and surgical referral centres, which challenges coherence and communication for the individual treatment decisions. The research project will be performed as a randomized controlled trial (RCT) with a 1-year inclusion period and two years of follow-up.
Age
18 - 120 years
Sex
ALL
Healthy Volunteers
No
Department of Physiotherapy, Univesity Hospital Gentofte
Gentofte Municipality, Hellerup, Denmark
Genoptræning og Rehabilitering, Rødovre Kommune
Rødovre Municipality, Rødovre, Denmark
Privathospitalet Danmark
Charlottenlund, Denmark
Department of rehabilitation, Gentofte Kommune
Hellerup, Denmark
Division of shoulder and elbow surgery, Department of orthopaedics, Univesity Hospital Gentofte
Hellerup, Denmark
Mit Lægehus
Rødovre Municipality, Denmark
Start Date
August 12, 2024
Primary Completion Date
September 1, 2030
Completion Date
September 1, 2030
Last Updated
April 2, 2025
1,000
ESTIMATED participants
Systematic use of patient reported outcome measures in clinical work with the patients
OTHER
Lead Sponsor
University Hospital, Gentofte, Copenhagen
Collaborators
NCT06381791
NCT06195956
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06319911